Abstract: The invention relates to a pigment with a metallic luster, comprising a plate-like non-metallic substrate having a thickness lower an 200 nm, which is entirely coated with a metallic layer.
Type:
Grant
Filed:
September 27, 2002
Date of Patent:
February 14, 2006
Assignee:
Merck Patent GmbH
Inventors:
Gerhard Pfaff, Stephanie Andes, Michael Uhlig
Abstract: The subject of the present invention is the use of the ROR receptors and/or of their response element or alternatively of a functional equivalent thereof for the screening of substances having antiatherosclerotic properties. The invention also relates to the methods of screening substances having antiatherosclerotic properties using the ROR receptors and/or their response elements. The invention also relates to the use of the methods of screening according to the present invention in order to characterize, justify and claim the mechanism of action of substances having antiatherosclerotic properties using the ROR receptors and/or their response elements as well as their effects on apo C-III.
Abstract: Compounds of formula (I) are disclosed. The compounds inhibit the action of gamma secretase, and hence find use in the treatment and prevention of Alzheimer's disease.
Type:
Grant
Filed:
August 8, 2001
Date of Patent:
February 7, 2006
Assignee:
Merck Sharp & Dohme Limited
Inventors:
Ian Churcher, Alan John Nadin, Andrew Pate Owens
Abstract: Nucleic acids, including DNA constructs and RNA transcripts, capable of inducing coordinate expression of two to three cistrons upon direct introduction into animal tissues, are bi- or tri-cistronic polynucleotides of this invention include those encoding and co-expressing HIV gene products, genes encoding antigens unrelated to HIV, and immunostimulatory gene products, including but not limited to GM-CSF, interleukins, interferon and members of the B7 family of proteins which act as T-cell costimulatory elements. The methods and polynucleotides of this invention are generally applicable to co-ordinate expression in vivo of any two or more genes in a single cell.
Type:
Grant
Filed:
September 10, 1999
Date of Patent:
February 7, 2006
Assignee:
Merck & Co., Inc.
Inventors:
Margaret A. Liu, John W. Shiver, Helen C. Perry
Abstract: ANIC-BP-1B polypeptides and polynucleotides and methods for producing such polypeptides by recombinant techniques are disclosed. Also disclosed are methods for utilizing ANIC-BP-1B polypeptides and polynucleotides in diagnostic assays.
Abstract: The invention relates to a dry chemical method and a test strip for determining calcium and magnesium in aqueous samples. Said test strip contains o-cresolphthalein complex (o-CPC; CAS Registry No. 2411-89-4) as a colour-causing reagent in a buffer system with a pH value of below 8.5. By using in particular an aqueous ethanolic imidazole buffer with a pH value of 6.75, conditions can be set up in such a way that the o-CPC has an identical molar sensitivity with respect to Ca and Mg. The total water hardness of aqueous samples can thus be easily determined.
Abstract: The invention relates to a process of preparing films and multilayers comprising polymerized liquid crystal material with uniform orientation, to films and multilayers obtained by said process and their use for optical and electrooptical applications.
Abstract: Disclosed are compositions and methods for producing fusion proteins with reduced immunogenicity. Fusion proteins of the invention include a junction region having an amino acid change that reduces the ability of a junctional epitope to bind to MHC Class II, thereby reducing its interaction with a T-cell receptor. Methods of the invention involve analyzing, changing, or modifying one or more amino acids in the junction region of a fusion protein in order to identify a T-cell epitope and reduce its ability to interact with a T cell receptor. Compositions and methods of the invention are useful in therapy.
Type:
Application
Filed:
September 23, 2005
Publication date:
February 2, 2006
Applicant:
MERCK Patent GmbH
Inventors:
Stephen Gillies, Jeffrey Way, Anita Hamilton
Abstract: Human Papillomavirus virus like particles (VLPs) have been constructed so that they contain a modified L2 protein. The L2 protein has been minimized and is fused to a second protein or peptide. The fused protein is incorporated into the VLP and the VLP can deliver the protein to a cell. The modified VLPs can be used to increase the breadth of immune response in vaccine preparations or to deliver other proteins of interest.
Type:
Grant
Filed:
August 10, 1999
Date of Patent:
January 31, 2006
Assignee:
Merck & Co., Inc.
Inventors:
Robert S. Lowe, Kathrin U. Jansen, Joseph G. Joyce, William L. McClements, James C. Cook, III, Jessica Ching-Yee Ling, Michael P. Neeper
Abstract: A method for managing the treatment regimen of a human patient using an over-the-counter (OTC) medicine is provided. The method comprises providing to the patient an interactive therapy managing system for de-selecting himself from the treatment regimen. The interactive therapy managing system may comprise, for example, an in person contact, or an electronically enabled element, such as an automated voice response system, a text-messaging system, an email system, a touch-tone telephone menu system, and a website.
Type:
Application
Filed:
July 20, 2005
Publication date:
January 26, 2006
Applicants:
McNeil-PPC, Inc., Merck & Co., Inc.
Inventors:
Lisa Berry, Jerry Hansen, Robert Hasselman, Alexandra Langendorfer, Stephanie Levy
Abstract: This interspinous vertebral implant comprises a body (11) which is intended to be inserted between two consecutive interspinous processes (3, 4), is compressible in the direction of the spine and is provided with means for anchoring it to at least one spinous process. The body (11) is formed by a single loop closed upon itself. The anchoring means are formed by two fixing lugs (12, 13) which are integral with the body (11), extend on either side of the spinous process in the area of which they are intended to anchor when the implant is in place, and are each traversed by a through-opening (14, 15) oriented in a direction substantially perpendicular to the general plane of said process, the through-openings being intended to receive fixing studs (23) to be crimped in the area of the process in question.
Abstract: Novel sulphones of formula I are disclosed: The compounds modulate the processing of amyloid precursor protein by gamma-secretase, and hence are useful in the treatment or prevention of Alzheimer's disease.
Type:
Grant
Filed:
August 20, 2002
Date of Patent:
January 10, 2006
Assignee:
Merck Sharp & Dohme Limited
Inventors:
Ian Churcher, Kevin Dinnell, Timothy Harrison, Sonia Kerrad, Alan John Nadin, Paul Joseph Oakley, Duncan Edward Shaw, Martin Richard Teall, Susannah Williams, Brian John Williams
Abstract: A class of compounds is disclosed which are diasteroisomers of a known class of protease inhibitors. The compound inhibit gamma-secretase, and find use in the treatment of and/or prevention of Alzheimer's disease.
Type:
Grant
Filed:
April 4, 2001
Date of Patent:
January 10, 2006
Assignee:
Merck, Sharp & Dohme Ltd.
Inventors:
Alan John Nadin, Graeme Irvine Stevenson
Abstract: The present invention relates to new fusion proteins which consist of a tumor-associated targeting element preferentially a monoclonal antibody or a fragment thereof recognizing a molecule which is preferentially expressed on human tumor cells such as the human epidermal growth factor receptor (EGFR), and a biologically active ligand such as a growth and/or differentiation factor. The resulting fusion protein may be used to deliver the biologically active ligand to a specific target cell or tissue. The new immunoconjugates can be used in tumor therapy.
Type:
Grant
Filed:
December 23, 1994
Date of Patent:
December 27, 2005
Assignee:
Merck Patent GmbH
Inventors:
Ilka von Hoegen, Uwe Hofmann, Carlota-Silvia Jaggle, Wolfgang Strittmatter, Jörg Stadlmüller, Siegfried Matzku
Abstract: The present invention is directed to a pharmaceutical composition comprising a compound of Formula I dissolved in propylene glycol and water. The present invention also relates to a pharmaceutical composition containing a compound of Formula I dissolved in propylene glycol and a buffer that has a pH between about 3 and about 5.
Type:
Grant
Filed:
September 26, 2002
Date of Patent:
December 27, 2005
Assignees:
Merck & Co., Inc., Banyu Pharmaceutical Co., Ltd.
Inventors:
Yuichi Sato, David T. Breslin, Shyam B. Karki
Abstract: A blister package for a pharmaceutical treatment card suitable, the blister package having a plurality of individual blisters suitable for containing a pre-measured dosage of a pharmaceutical composition in the form of tablets, pills and capsules. In accordance with a pre-determined schedule of administration of the individually sealed blisters may be opened by a method of tearing, peeling and pushing. The blister card package can be characterized as a multiple layer laminate assembly having a plurality of transparent cavities containing composition.
Abstract: The invention relates to a photostable liquid-crystalline medium comprising at least one compound of the formula I and at least one compound of the formula II and to the use thereof for electro-optical purposes, and to displays containing this medium.
Type:
Application
Filed:
September 25, 2003
Publication date:
December 22, 2005
Applicant:
Merck Patent GmbH
Inventors:
Atsutaka Manabe, Ulrich Heywang, Detlef Pauluth, Michael Heckmeier, Peer Kirsch, Elvira Montenegro
Abstract: Tetrahydropyran derivatives having at least one ester group (—CO—O—) and at least one group —CN, —NCS, —F, —Cl, —OCHF2, —OCF3, —CF3, —OCHFCF3, —OCF2CHFCF3, SF5, or —OCF2CF3; a process for preparing said tetrahydropyran derivatives, and the use of said tetrahydropyran derivatives as a component in a liquid crystal composition.
Type:
Grant
Filed:
May 27, 2004
Date of Patent:
December 13, 2005
Assignee:
Merck Patent GmbH
Inventors:
Mark John Goulding, Warren Duffy, Kevin Adlem, Peer Kirsch, Alexander Hahn, Eike Poetsch, Werner Binder, Volker Meyer, Melanie Klasen-Memmer, Michael Heckmeier, Georg Lüssem
Abstract: The invention relates to a non-dusting homogeneous pigment preparation notable in that it comprises at least 40% by weight of one or more effect pigments, from 0.5 to 50% by weight of water and/or an organic solvent or solvent mixture and from 0.5 to 59.5% by weight of a styrene-modified polyacrylate resin having an acid number >90 mg KOH/g, and to its use to produce dry preparations.
Type:
Grant
Filed:
June 13, 2000
Date of Patent:
December 6, 2005
Assignee:
Merck Patent GmbH
Inventors:
Carsten Griessmann, Gerhard Herget, Jochen Meyer, Thomas Rathschlag